| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33417922-33418051 | Rare:49 | ||||
| chr6:34696768-34696972 | Common:1; Rare:45 | ||||
| chr6:34757331-34757550 | Common:1; Rare:66 | ||||
| chr6:42879585-42879933 | Rare:100 | ||||
| chr6:42929240-42929556 | Common:3; Rare:85 | ||||
| chr6:42984319-42984619 | Rare:75 | ||||
| chr6:43013841-43014283 | Common:2; Rare:108 | ||||
| chr6:43516869-43517102 | Common:3; Rare:91; Clinvar:2 | ||||
| chr6:44127355-44127623 | Common:4; Rare:75 | ||||
| chr6:49463186-49463366 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995341-52995812 | Common:4; Rare:201 | ||||
| chr6:53348926-53349222 | Common:2; Rare:95 | ||||
| chr6:57172544-57172696 | Common:1; Rare:50 | ||||
| chr6:69866500-69866578 | Common:1; Rare:13 | ||||
| chr6:73523801-73523860 | Rare:18 |